Evidence map›Paper›PMID 35563552›Full record

ArticleInternational journal of molecular sciences2022

Is Infantile Hemangioma a Neuroendocrine Tumor?

Priscilla Kaulanjan-Checkmodine, Sandra Oucherif, Sorilla Prey, Etienne Gontier, Sabrina Lacomme, Maya Loot, Marijana Miljkovic-Licina, Muriel Cario, Christine Léauté-Labrèze, Alain Taieb and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Observational
  3. Article
  4. Article
  5. Review
  6. Infantile hemangioma models: is the needle in a haystack?Journal of translational medicine · 2023
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 2 countries.

Priscilla Kaulanjan-CheckmodineBRIC, UMR 1312, Inserm, University Bordeaux, F-33076 Bordeaux, France.
Sandra OucherifBRIC, UMR 1312, Inserm, University Bordeaux, F-33076 Bordeaux, France.ORCID 0000-0001-6462-4363
Sorilla PreyBRIC, UMR 1312, Inserm, University Bordeaux, F-33076 Bordeaux, France.
Etienne GontierElectron Microscopy Unit, Bordeaux Imaging Center, F-33076 Bordeaux, France.
Sabrina LacommeElectron Microscopy Unit, Bordeaux Imaging Center, F-33076 Bordeaux, France.ORCID 0000-0003-0752-1362
Maya LootCHU de Bordeaux, Service de Chirurgie Pédiatrique, F-33000 Bordeaux, France.
Marijana Miljkovic-LicinaDepartment of Pathology and Immunology, University of Geneva Medical School, Rue Michel-Servet 1, CH-1211 Geneva, Switzerland.ORCID 0000-0001-9023-2208
Muriel CarioBRIC, UMR 1312, Inserm, University Bordeaux, F-33076 Bordeaux, France.
Christine Léauté-LabrèzeBRIC, UMR 1312, Inserm, University Bordeaux, F-33076 Bordeaux, France.
Alain TaiebBRIC, UMR 1312, Inserm, University Bordeaux, F-33076 Bordeaux, France.ORCID 0000-0002-0928-8608
François MoisanBRIC, UMR 1312, Inserm, University Bordeaux, F-33076 Bordeaux, France.ORCID 0000-0003-2680-7497
Hamid Reza RezvaniBRIC, UMR 1312, Inserm, University Bordeaux, F-33076 Bordeaux, France.
Inserm · FRUniversité de Bordeaux · FRCentre Hospitalier Universitaire de Bordeaux · FRUniversity of Geneva · CH

Funding

Agence Nationale de la Recherche ANR-12-BSV1-0021-01
6 · The paper itself

Abstract

Infantile hemangioma (IH) is the most common infantile tumor, affecting 5-10% of newborns. Propranolol, a nonselective β-adrenergic receptor (ADRB) antagonist, is currently the first-line treatment for severe IH; however, both its mechanism of action and its main cellular target remain poorly understood. Since betablockers can antagonize the effect of natural ADRB agonists, we postulated that the catecholamine produced in situ in IH may have a role in the propranolol response. By quantifying catecholamines in the IH tissues, we found a higher amount of noradrenaline (NA) in untreated proliferative IHs than in involuted IHs or propranolol-treated IHs. We further found that the first three enzymes of the catecholamine biosynthesis pathway are expressed by IH cells and that their levels are reduced in propranolol-treated tumors. To study the role of NA in the pathophysiology of IH and its response to propranolol, we performed an in vitro angiogenesis assay in which IH-derived endothelial cells, pericytes and/or telocytes were incorporated. The results showed that the total tube formation is sensitive to propranolol only when exogenous NA is added in the three-cell model. We conclude that the IH's sensitivity to propranolol depends on crosstalk between the endothelial cells, pericytes and telocytes in the context of a high local amount of local NA.

Indexed as

HemangiomaNeuroendocrine TumorsAdrenergic beta-AntagonistsEndothelial CellsHumansInfantInfant, NewbornNorepinephrinePropranololAdrenergic beta-AntagonistsNorepinephrinePropranololadrenergicbetablockercatecholamineshemangiomapropranololtelocytes

Identifiers

PMID35563552
PMCPMC9104933
OpenAlexW4229449223

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.